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Terbutaline Sulfate
Terbutaline Sulfate - 17478-933-01 - (Terbutaline Sulfate)
Drug Information of Terbutaline Sulfate
| Product NDC: | 17478-933 |
| Proprietary Name: | Terbutaline Sulfate |
| Non Proprietary Name: | Terbutaline Sulfate |
| Active Ingredient(s): | 1 mg/mL & nbsp; Terbutaline Sulfate |
| Administration Route(s): | SUBCUTANEOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Terbutaline Sulfate
| Product NDC: | 17478-933 |
| Labeler Name: | Akorn |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078151 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20100201 |
Package Information of Terbutaline Sulfate
| Package NDC: | 17478-933-01 |
| Package Description: | 10 AMPULE in 1 CARTON (17478-933-01) > 1 mL in 1 AMPULE |
NDC Information of Terbutaline Sulfate
| NDC Code | 17478-933-01 |
| Proprietary Name | Terbutaline Sulfate |
| Package Description | 10 AMPULE in 1 CARTON (17478-933-01) > 1 mL in 1 AMPULE |
| Product NDC | 17478-933 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Terbutaline Sulfate |
| Dosage Form Name | INJECTION |
| Route Name | SUBCUTANEOUS |
| Start Marketing Date | 20100201 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn |
| Substance Name | TERBUTALINE SULFATE |
| Strength Number | 1 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
